Matches in Nanopublications for { ?s ?p "[Expansions of a hexanucleotide repeat (GGGGCC) in the noncoding region of the C9ORF72 gene are the most common cause of the familial form of ALS (C9-ALS), as well as frontotemporal lobar degeneration and other neurological diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Expansions of a hexanucleotide repeat (GGGGCC) in the noncoding region of the C9ORF72 gene are the most common cause of the familial form of ALS (C9-ALS), as well as frontotemporal lobar degeneration and other neurological diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Expansions of a hexanucleotide repeat (GGGGCC) in the noncoding region of the C9ORF72 gene are the most common cause of the familial form of ALS (C9-ALS), as well as frontotemporal lobar degeneration and other neurological diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1122007.RAqMhPuzqZ_J146Xeo0TfMPLTfu3gHECXJu-FHICtxhic130_assertion description "[Expansions of a hexanucleotide repeat (GGGGCC) in the noncoding region of the C9ORF72 gene are the most common cause of the familial form of ALS (C9-ALS), as well as frontotemporal lobar degeneration and other neurological diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1122007.RAqMhPuzqZ_J146Xeo0TfMPLTfu3gHECXJu-FHICtxhic130_provenance.
- NP979969.RA_FUy8_RgCWokRviSuJAW5Swb9pNovqkaONaf1Zoqc5w130_assertion description "[Expansions of a hexanucleotide repeat (GGGGCC) in the noncoding region of the C9ORF72 gene are the most common cause of the familial form of ALS (C9-ALS), as well as frontotemporal lobar degeneration and other neurological diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP979969.RA_FUy8_RgCWokRviSuJAW5Swb9pNovqkaONaf1Zoqc5w130_provenance.
- NP980012.RA3Kulen_89CIPWXuEXdpnIkE-Z8xCfqYC4VizHW1O2vk130_assertion description "[Expansions of a hexanucleotide repeat (GGGGCC) in the noncoding region of the C9ORF72 gene are the most common cause of the familial form of ALS (C9-ALS), as well as frontotemporal lobar degeneration and other neurological diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP980012.RA3Kulen_89CIPWXuEXdpnIkE-Z8xCfqYC4VizHW1O2vk130_provenance.
- NP1122008.RA3wyUuFigGEM6bMmJibNOXkR8qx228cL12lkHb0o9B-8130_assertion description "[Expansions of a hexanucleotide repeat (GGGGCC) in the noncoding region of the C9ORF72 gene are the most common cause of the familial form of ALS (C9-ALS), as well as frontotemporal lobar degeneration and other neurological diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1122008.RA3wyUuFigGEM6bMmJibNOXkR8qx228cL12lkHb0o9B-8130_provenance.